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T10732Tematropium；化合物TematropiumCDDD3602|||Tematropium metilsulfate|||HGP6；CDDD3602|||Tematropium metilsul
Tematropium (CDDD3602) possesses anticholinergic effects and can be used in neurological studies.
价 格：￥电议型 号：T10732产 地：中国大陆
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T10719CCT365623 hydrochloride；化合物 T10719CCT365623 hydrochloride
CCT365623 hydrochloride is an orally active inhibitor of lysyl oxidase (LOX) (IC50: 0.89 μM). It suppresses EGFR (pY1068) and AKT phosphorylation driven by EGF.
价 格：￥电议型 号：T10719产 地：中国大陆
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T106365α-reductase-IN-1；化合物 T106365α-reductase-IN-1
5α-reductase-IN-1 is a potent inhibitor of the enzyme 5α-reductase. This compound is primarily employed in research studies to investigate its potential efficacy in treating patterned alopecia. It is commonly used in combination with minoxidil, a well-known treatment for hair loss.
价 格：￥电议型 号：T10636产 地：中国大陆
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T1057Azilsartan；阿齐沙坦TAK-536；TAK-536|||阿齐沙坦
Azilsartan (TAK-536) is an Angiotensin 2 Receptor Blocker. The mechanism of action of azilsartan is as an Angiotensin 2 Type 1 Receptor Antagonist. The physiologic effect of azilsartan is by means of Decreased Blood Pressure.
价 格：￥电议型 号：T1057产 地：中国大陆
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T10556BKI-1369；化合物 T10556BKI-1369
BKI-1369 is a bumped kinase inhibitor. BKI-1369 increases hERG-inhibitory activity (IC50:1.52 μM).
价 格：￥电议型 号：T10556产 地：中国大陆
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T10536BI 703704；化合物 T10536BI 703704
BI 703704, a soluble guanylate cyclase (sGC) activator, inhibits the progression of diabetic nephropathy in the ZSF1 rat [1].
价 格：￥电议型 号：T10536产 地：中国大陆
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T10495LBefiradol化合物 T10495LNLX-112|||F13640
Befiradol (NLX-112) is an agonist of 5-HT1A receptor.
价 格：￥电议型 号：T10495L产 地：中国大陆
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T10440Azilsartan-d5；化合物 T10440TAK-536 D5；TAK-536 D5
Azilsartan (TAK-536) D5 is the deuterium-labeled Azilsartan. Azilsartan is a specific antagonist of the angiotensin II type 1 receptor.
价 格：￥电议型 号：T10440产 地：中国大陆
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T10436LAZD4573 HCl (2057509-72-3 free base)；化合物 T10436LAZD4573 hydrochloride|||AZD4573|||AZD4573 HCl|||AZD-
AZD-4573 is a selective and short-acting inhibitor of the serine/threonine cyclin-dependent kinase 9, the catalytic subunit of the RNA polymerase II elongation factor positive transcription elongation factor b. It also has a potential antineoplastic activity.
价 格：￥电议型 号：T10436L产 地：中国大陆
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T10436AZD4573；化合物AZD4573AZD4573
AZD4573 is an effective and selective CDK9 inhibitor (IC50: <4 nM). It enables transient target engagement for the treatment of hematologic malignancies.
价 格：￥电议型 号：T10436产 地：中国大陆
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T10429Tizaterkib；化合物AZD-0364AZD-0364；AZD-0364
Tizaterkib (AZD-0364) is a potent and selective ERK2 inhibitor.
价 格：￥电议型 号：T10429产 地：中国大陆
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T10382AS2863619 free base；化合物 T10382AS2863619 free base
AS2863619 free base enables the conversion of antigen-specific effector/memory T cells into Foxp3+ regulatory T (Treg) cells. It is a potent, orally active CDK8 and CDK19 inhibitor (IC50s: 0.61 nM and 4.28 nM). STAT5 activation enhanced by AS2863619 free base inhibition of CDK8/19, which consequently activates the Foxp3 gene.
价 格：￥电议型 号：T10382产 地：中国大陆
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T10369Aristeromycin；化合物 T10369Aristeromycin
Aristeromycin is an adenosine analog and an antibiotic and. It is a potent S-adenosylhomocysteine hydrolase (AHCY) inhibitor.
价 格：￥电议型 号：T10369产 地：中国大陆
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T10368Aripiprazole (D8)；化合物 T10368OPC-14597u00A0D8；OPC-14597u00A0D8
Aripiprazole D8 (OPC-14597 D8) is the deuterium-labeled Aripiprazole. Aripiprazole is a human 5-HT1A receptor partial agonist (Ki: 4.2 nM).
价 格：￥电议型 号：T10368产 地：中国大陆
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T10367Arginase inhibitor 1；化合物 T10367Arginase inhibitor 1
Arginase inhibitor 1 is a potent inhibitor of human arginases I and II (IC50s: 223 and 509 nM).
价 格：￥电议型 号：T10367产 地：中国大陆
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T10366LArg-Gly-Asp-Ser acetate；化合物Arg-Gly-Asp-Ser acetateArg-Gly-Asp-Ser acetate(91037-65-9 free base)；Arg-
Arg-Gly-Asp-Ser acetate is an integrin binding sequence that directly and specifically bind pro-caspase-8, pro-caspase-9 and pro-caspase-3, while it does not bind pro-caspase-1. Arg-Gly-Asp-Ser acetate inhibits integrin receptor function.
价 格：￥电议型 号：T10366L产 地：中国大陆
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T10366Arg-Gly-Asp-Ser化合物 T10366Fibronectin tetrapeptide|||RGDS peptide
Arg-Gly-Asp-Ser is an integrin-binding sequence that inhibits integrin receptor function. It decreases systemic inflammation via inhibition of collagen-triggered activation of leukocytes and attenuates expression of inflammatory cytokines, MMP-9, and iNOS.
价 格：￥电议型 号：T10366产 地：中国大陆
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T10364Arbutamine；阿布他明GP 21213；GP 21213
Arbutamine (GP 21213) is a novel potent non-selective beta-adrenoceptor agonist with alpha-1-sympathomimetic activity.Arbutamine promotes cardiac stress and increases heart rate, cardiac contractility.Arbutamine can be used to study cardiac stress and coronary artery disease
价 格：￥电议型 号：T10364产 地：中国大陆
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T10363Arazine；化合物ArazineN-Acetyl-S-farnesyl-L-cysteine；N-Acetyl-S-farnesyl-L-cysteine
Arazine (N-Acetyl-S-farnesyl-L-cysteine) can be a a substrate for isoprenylcysteine methyltransferase by competing with prenylated G protein or its receptors site. Arazine is a cell-permeable modulator of G protein and GPCR signaling.
价 格：￥电议型 号：T10363产 地：中国大陆
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T10362LAR453588 hydrochloride；化合物 T10362LAR453588 hydrochloride
AR453588 hydrochloride is an orally bioavailable anti-diabetic glucokinase activator (EC50: 42 nM) with anti-hyperglycemic activity.
价 格：￥电议型 号：T10362L产 地：中国大陆
